Nitroaniline derivatives and their use as anti-tumour agents

ABSTRACT

The invention provides nitroaniline derivatives represented by general formula (I) where the nitro group is substituted at any one of the available benzene positions 2-6; where R and A separately represent the groups NO 2 , CN, COOR 1 , CONR 1  R 2 , CSNR 1  R 2  or SO 2  NR 1  R 2  and A is substituted at any one of the available benzene positions 2-6; where B represents N(CH 2  CH 2  halogen) 2  or N(CH 2  CH 2  OSO 2  R 3 ) 2  substituted at any one of the available benzene positions; and where R 1 , R 2  and R 3  separately represent H, or lower alkyl optionally substituted with hydroxyl, ether, carboxy or amino functions, including cyclic structures, or R 1  and R 2  together with the nitrogen form a heterocyclic structure, and pharmaceutical preparations containing them. These compounds have activity as hypoxia-selective cytotoxins, reductively-activated prodrugs for cytotoxins, hypoxic cell radiosensitisers, and anticancer agents.

This application is a 371 of PCT/GB92/02199 filed Nov. 27, 1992.

Alkylating agents are an important class of anticancer drugs, which express their cytotoxic and antitumour effects by forming adducts with cellular DNA (Garcia et al., Biochem. Pharmacol., 1988, 37, 3189).

The present invention relates to novel nitroaniline-based alkylating agents having activity as hypoxia-selective cytotoxins, reductively-activated prodrugs for cytotoxins, hypoxic cell radiosensitisers, and anticancer agents, to methods of preparing the novel compounds, and to the use of these compounds as antitumour agents.

In one aspect, the present invention relates to the class of nitroaniline derivatives represented by the general formula (I); ##STR2## where the nitro group is substituted at any one of the available benzene positions 2-6; where R and A separately represent the groups NO₂, CN, COOR¹, CONR¹ R², CSNR¹ R² or SO₂ NR¹ R² and A is substituted at one of the available benzene positions 2-6; where B represents N(CH₂ CH₂ halogen)₂ or N(CH₂ CH₂ OSO₂ R³)₂ substituted at any one of the available benzene positions; and where R¹, R² and R³ separately represent H, or lower alkyl optionally substituted with hydroxyl, ether, carboxyl or amino functions, including cyclic structures, or R¹ and R² together with the nitrogen form a heterocyclic structure.

Where R¹, R² and/or R³ represent lower alkyl, the group may contain from 1 to 6 carbon atoms.

Where R¹, R² and/or R³ represent groups containing tertiary amines, the N-oxides of those tertiary amine moieties are also included.

The compounds of formula (I) have cytotoxic and antitumour activity, and are useful as hypoxia-selective cytotoxins, reductively-activated prodrugs for cytotoxins, hypoxic cell radiosensitisers, and anticancer agents.

Some of the compounds of formula (I) form pharmaceutically-acceptable addition salts with both organic and inorganic acids, and these addition salts also form part of the present invention. Examples of suitable acids for salt formation are hydrochloric, sulfuric, phosphoric, acetic, citric, oxalic, malonic, salicylic, malic, fumaric, succinic, ascorbic, maleic, methanesulfonic, isethionic and the like. Some of the compounds of formula (I) form pharmaceutically-acceptable addition salts with both organic and inorganic bases, and these addition salts also form part of the present invention. Examples of suitable bases for salt formation are sodium and potassium carbonate, sodium and potassium hydroxide, ammonia, triethylamine, triethanolamine and the like.

The compounds of formula (I) and the acid or base addition salts and the N-oxides thereof may be prepared by the processes outlined in the following Schemes 1 to 7.

Specific but non-limitative examples of the processes outlined in Schemes 1 to 7 are given hereinafter in Examples A to H respectively. ##STR3##

The invention also relates to the preparation of compounds of the general formula I, the acid or base addition salts and the N-oxides thereof, by a process as outlined in any one of Schemes 1-7 above or by an obvious chemical equivalent thereof. The invention includes also those forms of the preparation processes according to which a compound obtainable as intermediate at any stage of the process is used as starting material and the remaining steps are carried out, or a starting material is used in the form of a derivative or salt or, especially, is formed under the reaction conditions.

The following Table 1 sets out physiochemical data for 24 compounds within the general formula (I), representative of it, and preparable by the processes of the invention.

                                      TABLE 1                                      __________________________________________________________________________     Analytical and physicochemical data for nitroaniline mustards of general       formula 1.                                                                     No.                                                                               A    NO.sub.2                                                                          B           R              mp (°C.)                                                                      formula      analyses.sup.a        __________________________________________________________________________     1  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH.sub.2     109-111                                                                              C.sub.11 H.sub.12 Cl.sub.2                                                     N.sub.4 O.sub.5                                                                             C,H,N,Cl              2  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Br).sub.2                                                            CONH.sub.2     126-128                                                                              C.sub.11 H.sub.12 Br.sub.2                                                     N.sub.4 O.sub.5                                                                             C,H,N                 3  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 I).sub.2                                                             CONH.sub.2     170-172                                                                              C.sub.11 H.sub.12 I.sub.2                                                      N.sub.4 O.sub.5                                                                             C,H,N,I               4  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 OMs).sub.2.sup.b                                                     CONH.sub.2     142-144                                                                              C.sub.11 H.sub.18 N.sub.4                                                      O.sub.11 S.sub.2                                                                            C,H,N,S               5  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            COOMe          136.5-138                                                                            C.sub.12 H.sub.13 Cl.sub.2                                                     N.sub.3 O.sub.6                                                                             C,H,N,Cl              6  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            COOH           125-127                                                                              C.sub.11 H.sub.11 Cl.sub.2                                                     N.sub.3 O.sub.6.1/2EtOAc                                                                    C,H,N                 7  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CN             127   C.sub.11 H.sub.10 Cl.sub.2                                                     N.sub.4 O.sub.4                                                                             C,H,N                 8  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONHMe         180.5 C.sub.12 H.sub.14 Cl.sub.2                                                     N.sub.4 O.sub.4                                                                             C,H,N,Cl              9  2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONMe.sub.2    130.5 C.sub.13 H.sub.16 Cl.sub.2                                                     N.sub.4 O.sub.5                                                                             C,H,N                 10 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONX.sup.c     140-142                                                                              C.sub.15 H.sub.18 Cl.sub.2                                                     N.sub.4 O.sub.6                                                                             C,H,N                 11 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 NMe.sub.2.HCl                                                            85-90 C.sub.15 H.sub.21 Cl.sub.2                                                     N.sub.5 O.sub.5.HCl                                                                         C,H,N                 12 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 NX.sup.c.HCl                                                             119-120                                                                              C.sub.17 H.sub.23 Cl.sub.2                                                     N.sub.5 O.sub.6.HCl                                                                         C,H,N,Cl              13 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CSNH.sub.2     166-167                                                                              C.sub.11 H.sub.12 Cl.sub.2                                                     N.sub.4 O.sub.4.S                                                                           C,H,N,Cl              14 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 N(O)Me.sub.2                                                             165-169                                                                              C.sub.15 H.sub.21 Cl.sub.2                                                     N.sub.5 O.sub.6.HCl                                                                         C,H,N,Cl              15 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 COOH                                                                     150-153                                                                              C.sub.14 H.sub.16 Cl.sub.2                                                     N.sub.4 O.sub.7                                                                             C,H,N                 16 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONHCH.sub.2 CH.sub.2 OH                                                                      157-158                                                                              C.sub.13 H.sub.16 Cl.sub.2                                                     N.sub.4 O.sub.6                                                                             C,H,N,Cl              17 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONHCH.sub.2 CH(OH)CH.sub.2 OH                                                                gum   C.sub.14 H.sub.18 Cl.sub.2                                                     N.sub.4 O.sub.7                                                                             C,H,N,Cl              18 2-NO.sub.2                                                                          4  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            SO.sub.2 NH.sub.2                                                                             153-154                                                                              C.sub.10 H.sub.12 Cl.sub.2                                                     N.sub.4 O.sub.6 S                                                                           C,H,N,S               19 3-NO.sub.2                                                                          5  2-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH.sub.2     123-124                                                                              C.sub.11 H.sub.12 Cl.sub.2                                                     N.sub.4 O.sub.5                                                                             C,H,N,Cl              20 3-NO.sub.2                                                                          5  2-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 NMe.sub.2                                                                115-118                                                                              C.sub.15 H.sub.21 Cl.sub.2                                                     N.sub.5 O.sub.5                                                                             C,H,N,Cl              21 2-NO.sub.2                                                                          6  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH.sub.2       141-141.5                                                                          C.sub.11 H.sub.12 Cl.sub.2                                                     N.sub.4 O.sub.5                                                                             C,H,N,Cl              22 2-NO.sub.2                                                                          6  5-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 NMe.sub.2.HCl                                                            180-182                                                                              C.sub.15 H.sub.21 Cl.sub.2                                                     N.sub.5 O.sub.5.HCl                                                                         C,H,N,Cl              23 3-NO.sub.2                                                                          5  4-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH.sub.2     113-116                                                                              C.sub.11 H.sub.12 Cl.sub.2                                                     N.sub.4 O.sub.5                                                                             C,H,N,Cl              24 3-NO.sub.2                                                                          5  4-N(CH.sub.2 CH.sub.2 Cl).sub.2                                                            CONH(CH.sub.2).sub.2 NMe.sub.2.HCl                                                            145-148                                                                              C.sub.15 H.sub.21 Cl.sub.2                                                     N.sub.5 O.sub.5.HCl.H.sub.2                                                                 C,H,N                 __________________________________________________________________________      Footnotes for TABLE 1                                                          .sup.a Analyses for all listed elements within ±0.4%.                       .sup.b OMs = OSO.sub.2 CH.sub.3.                                               .sup.c X = morpholide: (CH.sub.2 CH.sub.2).sub.2 O.                      

The following Examples A to H illustrate the preparation of compounds representative of the general formula (I), and specifically the compounds listed in Table 1.

EXAMPLE A Preparation of 5-[N,N-bis(2-methanesulfonoxyethyl)amino]-2,4-dinitrobenzamide (4) (Ia: X═OSO₂ Me; R═CONH₂) and analogues by the method outlined in Scheme 1.

Treatment of 5-chloro-2,4-dinitrobenzoic acid (II: Y═OH) [Goldstein, H.; Stamm, R. Helv. Chim. Acta., 1952, 35, 1330-1332] with SOCl₂ followed by ammonia gave 5-chloro-2,4-dinitrobenzamide (II: Y═NH₂), mp 210° C. (dec) [Goldstein, H.; Stamm, R. Helv. Chim. Acta., 1952, 35, 1330-1332 report mp 212° C.]. ¹ H NMR (CD₃ COCD₃) δ 8.68 (s, 1 H, H-3), 8.02 (s, 1 H, H-6), 7.50 (br, 2 H, CONH₂). This amide was heated with diethanolamine in dioxan to give 5-[N,N-bis(2-hydroxyethyl)]amino-2,4-dinitrobenzamide (III) (45% yield), mp (EtOAc) 176°-178° C. ¹ H NMR (CD₃ SOCD₃) δ 8.47 (s, 1 H, ArH3), 8.07, 7.73 (2 br, 2 H, CONH₂), 7.35 (s, 1 H, ArH6), 4.80 (m, 2 H, OH), 3.83-3.20 (m, 8 H, CH₂ N, CH₂ O). Anal. (C₁₁ H₁₄ N₄ O₇) C,H,N.

Methanesulfonyl chloride (5.17 ml, 0.067 mol) was added dropwise to a solution of the above amide diol (10.00 g, 0.032 mol) in dry pyridine (150 mL) at 0° C. After a further 10 minutes at 0° C., the solution was stirred at 20° C. for 30 minutes, and then volatiles were removed under reduced pressure at below 40° C. The residue was partitioned between EtOAc and water, and the organic residue was chromatographed on silica gel. Elution with EtOAc gave foreruns, followed by 5-[N,N-bis(2-methanesulfonoxyethyl)amino]-2,4-dinitrobenzamide (4) (Ia: X═OSO₂ Me; R═CONH₂) (11.05 g, 74%), mp (sealed tube: ex EtOAc/petroleum ether) 60° C., ¹ H NMR(DC₃ COCD₃) δ 8.54 (s, 1 H, H-3), 7.65 (s, 1 H, H-6), 4.49 (t, J=5.3 Hz, 4 H, CH₂ OSO₂ CH₃), 3.89 (t, J=5.3 Hz, 4 H, CH₂ N), 3.09 (s, 6 H, SO₂ CH₃), 2.90 (br s, NH₂). ¹³ C NMR δ 167.01 (CONH₂), 148.56 (C-5), 140.45, 138.44 (C-2,4), 138.57 (C-1), 124.92, 123.06 (C-3,6), 67.65 (CH₂ OSO₂ CH₃), 52.02 (CH₂ N), 37.23 (SO₂ CH₃). Anal. (C₁₃ H₁₈ N₄ O₁₁ S₂) C,H,N,S.

The above dimesylate (4) (15.0 g, 31.9 mol) was dissolved in dry DMF (150 mL). The solution was treated with solid LiCl (20 g), warmed to 100° C. with vigorous stirring for 1 h, and then concentrated to dryness. The residue was partitioned between EtOAc and water, and the organic portion was washed well with 3N HCl, worked up to give a waxy solid, and chromatographed on silica. Elution with EtOAc/petroleum ether (1:1) gave foreruns, while EtOAc/petroleum ether (3:2) gave 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (1) (Ia, X═Cl, R═CONH₂) (7.51 g, 67%) which crystallised from EtOAc/petroleum ether as small orange needles, m.p. 109°-111° C., ¹ H NMR (CD₃ COCD₃) δ 8.52 (s, 1H, H-3), 7.58 (s, 1H, H-6), 7.10 (br, 2H, CONH₂), 3.89-3.81 (m, 8H, NCH₂ CH₂ Cl). ¹³ C NMR δ 167.10 (CONH₂), 148.31 (C-5), 140.08 (C-2), 138.84 (C-1), 138.20 (C-4), 124.94, 122.24 (C-3,6), 54.25 (CH₂ N), 42.04 (CH₂ Cl) ^(M) /z 354,352,350 (M+, 2%), 303,301 (67,24%),222(25),185(26),171(29),100(74),65(25),63(56),56(57),36(100). Found M+354.0124; 352.0123; 350.0189. Anal. (C₁₁ H₁₂ Cl₂ N₄ O₅) C, H, N, I.

A solution of the above dimesylate (4) (1.00 g, 2.12 mmol) in dry DMF (50 mL) was treated with solid NaBr (10.0 g), warmed to 120° C. with vigorous stirring for 15 min, and then concentrated to dryness under reduced pressure. The residue was partitioned between EtOAc and water, and the organic portion was washed well with 3N HCl and worked up. Chromatography of the residue on silica and elution with EtOAc/petroleum ether (1:1) gave 5-[N,N-bis(2-bromoethyl)amino]-2,4-dinitrobenzamide (2) (Ia: X═Br, R═CONH₂) (0.73 g, 78% yield), mp (EtOAc/petroleum ether) 126°-128° C. ¹ H NMR (CD₃ COCD₃) δ 8.53 (s, 1 H, H-3), 7.58 (s, 1 H, H-6), 3.89 (t, J=6.6 Hz, 4 H, CH₂ N), 3.73 (t, J=6.6 Hz, 4 H, CH₂ Br), 2.93 (br, 2 H, CONH₂). ¹³ C NMR δ 167.20 (CONH₂), 147.89 (C-5), 140.06, 138.26 (C-2,4), 138.75 (C-1), 124.95, 122.30 (C-3,6), 54.11 (CH₂ N), 29.89 (CH₂ Br). Anal. (C₁₁ H₁₂ Br₂ N₄ O₅) C,H,N.

A similar reaction using NaI gave 5-[N,N-bis(2-iodoethyl)amino]-2,4-nitrobenzamide (3) (Ia: X═I, R═CONH₂) in 92% yield, mp (EtOAc/petroleum ether) 170°-172° C. ¹ H NMR (CD₃ COCD₃) δ 8.52 (s, 1 H, H-3), 7.55 (s, 1 H, H-6), 3.84 (t, J=7.2 Hz, 4 H, CH₂ N), 3.50 (t, J=7.2 Hz, 4 H, CH₂ Br), 2.88 (br, 2 H, CONH₂). ¹³ C NMR δ 167.09 (CONH₂), 147.17 (C-5), 140.08, 138.33 (C-2,4), 138.74 (C-1), 124.94, 122.31 (C-3,6), 54.89 (CH₂ N), 1.72 (CH₂ I). Anal. (C₁₁ H₁₂ I₂ N₄ O₅) C,H,N,I.

EXAMPLE B Methyl 5-[N,N-bis(2-cloroethyl)amino]-2,4-dinitrobenzoate (5) (VI: X═Cl) and analogues by the method outlined in Scheme 2

Methyl 5-chloro-2,4-dinitrobenzoate (IV) (1.24 g, 4.76 mmol) was treated with diethanolamine (1.00 g, 9.52 mmol) in dioxane (50 mL) at 50° C. for 3 h, and the residue after workup was chromatographed on silica gel. Elution with EtOAc gave methyl 5-[N,N-bis(2-hydroxyethyl)amino]-2,4-dinitrobenzoate (V) (1.52 g, 97%), mp (EtOAc/petroleum ether) 104°-106° C. ¹ H NMR (CDCl₃) δ 8.48 (s, 1 H, H-3), 7.45 (s, 1 H, H-6), 3.95 (s, 3 H, OCH₃), 3.81 (t, J=5.0 Hz, 4 H, CH₂ OH), 3.60 (t, J=5.0 Hz, 4 H, CH₂ N), 2.20 (br, 2 H, OH). ¹³ C NMR δ 165.89 (COOMe), 147.53 (C-5), 138.67, 136.21 (C-2,4), 133.30 (C-1), 124.22, 121.65 (C-3,6), 59.34 (CH₂ OH), 54.59 (CH₂ N), 53.74 (OCH₃). Anal. (C₁₂ H₁₅ N₃ O₈) C,H,N.

A solution of this diol (1.50 g, 4.56 mmol) and Et₃ N (1.33 mL, 9.57 mmol) in dry CH₂ Cl₂ (60 mL) was treated with MsCl (0.73 mL, 9.34 mmol) at 0° C., and poured into saturated aqueous NaHCO₃ after 15 min. The crude dimesylate (VI; X═OSO₂ Me) from workup was treated directly with excess LiCl in DMF at 120° C. for 30 min. The mixture was poured into brine, extracted with EtOAc, worked up, and chromatographed on silica gel. Elution with EtOAc/petroleum ether gave methyl 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzoate (5) (VI: X═Cl; Y¹ ═OMe) (1.34 g, 80%), mp (EtOAc/petroleum ether) 136.5°-138° C. ¹ H NMR (CDCl₃) δ 8.54 (s, 1 H, H-3), 7.34 (s, 1 H, H-6), 3.97 (s, 3 H, OCH₃), 3.68 (br s, 8 H, NCH₂ CH₂ Cl). ¹³ C NMR δ 165.30 (COOCH₃), 147.22 (C5), 139.81, 137.82 (C-2,4), 133.39 (C-1), 124.33, 121.77 (C-3,6), 53.86 (OCH₃), 53.78 (CH₂ N), 40.69 (CH₂ Cl). Anal. (C₁₂ H₁₃ Cl₂ N₃ O₆) C,H,N,Cl.

Hydrolysis of (5) was 4N KOH in p-dioxane at 20° C. for 15 min gave a quantitative yield of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzoic acid (6) (Ib: X═Cl, R═COOH), mp (EtOAc/petroleum ether) 125°-127° C. ¹ H NMR (CD₃ COCD₃) δ 8.56 (s, 1H, H-3), 7.72 (s, 1 H, H-6), 3.89-3.86 (br, 8 H, NCH₂ CH₂ Cl), 3.78 (br, COOH). ¹³ C NMR δ 166.02 (COOH), 148.52 (C-5), 140.25, 138.09 (C-2,4), 134.72 (C-1), 124.87, 122.58 (C-3,6), 54.12 (CH₂ N), 42.12 (CH₂ Cl). Anal. (C₁₁ H₁₁ Cl₂ N₃ O₆.1/2EtOAc) C,H,N,Cl.

Treatment of (6) with excess SOCl₂ containing a drop of DMF under reflux for 20 min, followed by concentration to dryness and azeotroping with benzene, gave crude 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzoyl chloride (VI: X═Cl; Y¹ ═Cl). This was dissolved in Me₂ CO (20 mL), cooled to 0° C., treated with excess 40% aqueous methylamine. The product was purified by chromatography on silica gel, elution with EtOAc/petroleum ether (1:1) giving N-methyl [N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (8) (Ib: X═Cl, R═CONHMe), mp (EtOAc/petroleum ether) 180.5° C. ¹ H NMR (CD₃ COCD₃) δ 8.53 (s, 1 H, ArH3), 7.75 (br, 1 H, CONH), 7.56 (s, 1 H, H-6), 3.88-3.80 (m, 8 H, NCH₂ CH₂ Cl), 2.90, 2.89 (2 s, 3 H, CONHMe). ¹³ C NMR δ 165.89 (CONH), 148.43 (C-5), 140.05, 138.26 (C-2,4), 138.94 (C-1), 125.05, 122.45 (C-3,6), 54.20 (CH₂ N), 42.10 (CH₂ Cl), 26.69 (CONHCH₃). Anal. (C₁₂ H₁₄ Cl₂ N₄ O₅) C,H,N,Cl.

Similar treatment of the acid chloride (VI: X═Cl; Y¹ ═Cl) with ammonia or suitable amines gave:

5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (4) (Ib: X═Cl, R═CONH₂) (67% yield), mp (EtOAc/petroleum ether) 109°-111° C. ¹ H NMR (CD₃ COCD₃) δ 8.52 (s, 1 H, H-3), 7.58 (s, 1 H, H-6), 7.10 (br, 2 H, CONH₂), 3.89-3.81 (m, 8 H, NCH₂ CH₂ Cl). ¹³ C NMR δ 167.10 (CONH₂), 148.31 (C-5), 140.08 (C-2), 138.84 (C-1), 138.20 (C-4), 124.94, 122.24 (C-3,6), 54.25 (CH₂ N), 42.04 (CH₂ Cl). ^(M) /z 354, 352, 350 (M⁺, 2%), 303, 301 (67, 24%), 222 (25), 185 (26), 171(29), 100(74), 65(25), 63(56), 56(57), 36(100). Found M⁺ 354.0124; 352.0123; 350.0189. C₁₁ H₁₂ Cl₂ N₄ O₅ requires 354.0126; 352.0155; 350.0185. Anal. (C₁₁ H₁₂ Cl₂ N₄ O₅) C,H,N,Cl.

N,N-dimethyl [N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (9) (Ib: X═Cl, R═CONMe₂) (65% yield), mp (CHCl₃ /petroleum ether) 130.5° C. ¹ H NMR (CDCl₃) δ 8.61 (s, 1 H, H-3), 7.07 (s, 1 H, H-6), 3.62 (s, 8 H, NCH₂ CH₂ Cl), 3.07,2.78 (2×3 H, CON(CH₃)₂)). ¹³ C NMR δ 166.12 (CON(CH₃)₂)), 148.33 (C-5), 138.88, 135.75 (C-2,4), 137.82 (C-1), 124.92, 120.00 (C-3,6), 53.55 (CH₂ N), 40.98 (CH₂ Cl), 38.06, 34.85 (CON(CH₃)₂)). Anal. (C₁₃ H₁₆ Cl₂ N₄ O₅) C,H,N.

N-morpholino [N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (10) (Ib: X═Cl, R═CON(CH₂ CH₂)₂ O), mp (CHCl₃ /hexane) 140°-142° C. ¹ H NMR (CDCl₃) δ 8.66 (s, 1 H, ArH-3), 7.55 (s, 1 H, ArH-6), 3.68 (br, 10H, NCH₂ CH₂ Cl and CH₂ O), 3.60 & 3.34 (2×m, 2×2 H, CH₂ NCO). ¹³ C NMR δ 165.22 (CON), 149.34 (C-5), 139.88, 137.00 (C-2,4), 138.26 (C-1), 125.59, 121.17 (C-3,6), 66.92, 66.79 (CH₂ O), 54.22 (CH₂ N, 47.88, 42.80 (CONHCH₂), 42.26 (CH₂ Cl). Anal. (C₁₅ H₁₈ Cl₂ N₄ O₆) C,H,N.

N-[2-(dimethylamino)ethyl][N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (11) (Ib: X═Cl, R═CONHCH₂ CH₂ NMe₂), mp (hydrochloride salt from MeOH/EtOAc) 85°-90° C. ¹ H NMR (D₂ O) δ 8.76 (s, 1H, ArH-3), 7.59 (s, 1H, ArH-6), 3.86-3.80 (m, 10H, NCH₂ CH₂ Cl and CH₂ NH⁺ Me₂), 3.53 t, J=6.1 Hz, 2H, CONHCH₂), 3.06 (s, 6H, NMe₂). ¹³ C NMR δ 170.77 (CONH), 166.12, 1451.39 (C-5), 140.53, 137.51 (C-2,4), 138.18 (C-1), 128.25, 123.39 (C-3,6), 58.46 (CH₂ N⁺ HMe₂), 55.49 (CH₂ N), 45.67 (N⁺ HMe₂), 43.97 (CH₂ Cl), 38.54 (CONHCH₂). Anal. (C₁₅ H₂₁ Cl₂ N₅ O₅.HCl) C,H,N.

A solution of the free base of (11) (0.50 g, 1.18 mmol) in CH₂ Cl₂ (15 mL) was treated with a solution of 2-benzenesulfonyl-3-phenyloxaziridine [Davis, F.; Stringer, C. D. J. Org. Chem., 1982, 47, 1775-1777]. (0.32 g, 1.24 mmol) in CH₂ Cl₂ (3 mL) was added dropwise to. After 10 min, petroleum ether (10 mL) was added, the solution was cooled at -30° C. overnight, and the resulting solid was dried under high vacuum to give N-(N¹,N¹ -dimethylaminoethyl) [N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide N¹ -oxide (14) (Ib: X═Cl, R═CONHCH₂ CH₂ N(O)Me₂) as a hygroscopic foam. Treatment with MeOH/HCl gave the hydrochloride salt (0.36 g, 64%), mp (MeOH/^(i) Pr₂ O) 165°-169° C. ¹ H NMR (D₂ O/(CD₃)₂ SO) δ 8.82 (s, 1 H, H-3), 7.46 (s, 1 H, H-6), 3.98, 3.93 (2xt, J=5.1 Hz, 2×2 H, CH₂ CH₂), 3.82 (t, J=4.7 Hz, 4 H, CH₂ Cl), 3.77 (t, J=4.7 Hz, 4 H, CH₂ N), 3.57 (s, 6 H, N(CH₃)₂). ¹³ C NMR (D₂ O/(CD₃)₂ SO) δ 170.71 (CONH), 151.63 (C-5), 140.68, 137.31 (C-3,6), 69.20 (CH₂ NOMe₂), 59.03 (NOMe₂), 55.40 (CH₂ N), 44.06 (CH₂ Cl), 36.45 (CONH CH₂). Anal. (C₁₅ H₂₁ Cl₂ N₅ O₆.HCl) C,H,N,Cl.

N-[2-(morpholino)ethyl][N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (12) (Ib: X═Cl, R═CONHCH₂ CH₂ N(CH₂ CH₂)₂ O) as a gum. The hydrochloride salt crystallized from MeOH/^(i) Pr₂ O, mp 119°-120° C. ¹ H NMR (D₂ O) δ 8.81 (s, 1 H, H-3), 7.59 (s, 1 H, H-6), 4.07 (br, NH and HCl), 3.91 (t, J=6.0 Hz, 4 H, N⁺ CH₂ CH₂ O), 3.86-3.81 (m, 10 H, NCH₂ CH₂ Cl and CH₂ CH₂ N⁺), 3.56 (t, J=6.0 Hz, 6 H, N⁺ CH₂ CH₂ O and CONHCH₂). ¹³ C NMR δ 171.17 (CONH), 151.69 (C-5), 140.61, 137.28 (C-2,4), 138.12 (C-1), 128.53, 123.48 (C-3,6) 66.30 (N⁺ CH₂ C_(H) 2O), 58.07 (CH₂ N⁺), 55.48 (CH₂ N), 54.65 (N⁺ CH₂ CH₂ O), 44.09 (CH₂ Cl), 36.84 (CONHCH₂). Anal. (C₁₇ H₂₃ Cl₂ N₅ O₆.HCl.1/2H₂ O) C,H,N,Cl.

N-(2-hydroxyethyl) 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (16) (Ib: X═Cl, R═CONHCH₂ CH₂ OH) (1.24 g, 85%), mp (EtOAc/petroleum ether) 157°-158° C. ¹ H NMR ((CD₃)₂ SO) δ 8.73 t, J=5.5 Hz, 1 H, CONH), 8.53 (s, 1 H, H-3), 7.45 (s, 1 H, H-6), 4.76 (t, J=5.5 Hz, 1 H, OH), 3.82 (t, J=6.0 Hz, 4 H, CH₂ Cl), 3.68 (t, J=6.0 Hz, 4 H, CH₂ N), 3.54 (dt, J=6.1, 5.5 Hz, 2 H, CH₂ OH), 3.31 dt, J=6.1, 5.5 Hz, 2 H, CONHCH₂). ¹³ C NMR ((CD₃)SO) δ 164.44 (CONH), 147.11 (C-5), 137.87. 136.27 (C-2,4), 137.32 (C-1), 124.24, 121.01 (C-3,6), 59.32 (CH₂ OH), 52.44 (CH₂ N), 41.93 (CONHCH₂), 41.65 (CH₂ Cl). Anal. (C₁₃ H₁₆ Cl₂ N₂ O₆), C,H,N,Cl.

N-(2,3-dihydroxypropyl)5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (17) (Ib: X═Cl, R═CONHCH₂ CH(OH)CH₂ OH) (0.96 g, 59%) as a hygroscopic yellow foam. ¹ H NMR ((CD₃)₂ SO) δ 8.70 (t, J=5.7 Hz, 1 H, CONH), 8.53 (s, 1 H, H-3), 7.44 (s, 1 H, H-6), 4.83 (d, J=4.9 Hz, 1 H, CHOH) 4.56 (t, J=5.7 Hz, 1 H, CH₂ OH), 3.83 (t, J=5.9 Hz, 4 H, CH₂ Cl), 3.68 (t, J=5.9 Hz, 4 H, CH₂ N), 3.50-3.06 (m, 5 H, CONH CH₂ CHOHCH₂ OH). ¹³ C NMR ((CD₃)₂ SO) δ 164.61 (CONH), 147.12 (C-5), 37.94, 136.40 (C-2,4), 137.40 (C-1), 124.29, 121.18 (C-3,6). 70.08 (CHOH), 63.77 (CH₂ OH), 52.55 (CH₂ N), 42.79 (CONHCH₂), 41.72. (CH₂ Cl). Anal. (C₁₄ H₁₈ Cl₂ N₄ O₇) C,H,N,Cl.

crude N-(2-methoxycarbonylethyl) 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide [from treatment with β-alanine methyl ester hydrochloride] (Ib: X═Cl, R═CONHCH₂ CH₂ COOMe) as a yellow oil. This was immediately dissolved in THF (25 mL) and treated with aqueous KOH (10 mL of 2N) at 20° C. for 3 h. The solution was then acidified with conc. HCl, extracted with EtOAc, and worked up as usual. Chromatography on silica, eluting with EtOAc, gave N-(2-carboxyethyl) 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (15) (Ib: X═Cl, R═CONHCH₂ CH₂ COOH) (0.72 g, 68%), mp (EtOAc/petroleum ether) 150°-153° C. ¹ H NMR ((CD₃)₂ SO) δ 12.27 (br, 1 H, COOH) 8.79 (t, J=5.6 Hz, 1 H, CONH), 8.54 (s, 1 H, H-3), 7.42 (s, 1 H, H-6), 3.83 (t, J=6.0 Hz, 2 H, CH₂ Cl), 3.68 (t, J=6.0 Hz, 4 H, CH₂ N), 3.44 (dxt, J=6.9, 2 H, 5.6 Hz, CONHCH₂), 2.53 (t, J=6.9 Hz, 2 H, CH₂, COOH). ¹³ C NMR ((CD₃)₂ SO) δ 172.74 (COOH), 164.53 (CONH), 147.21 (C-5), 137.94, 136.13 (C-2,4), 137.29 (C-1), 124.37, 120.93 (C-3,6), 52.58 (CH₂ N), 41.72 (CH₂ Cl), 35.24, 33.19 (CONHCH₂ CH₂). Anal. (C₁₄ H₁₆ Cl₂ N₄ O₇) C,H,N,Cl.

EXAMPLE C Preparation of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzonitrile (7) (Ic: X═Cl, R═CN) and 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrothiobenzamide (13) (Ic: X═Cl, R═CSNH₂) by the method outlined in Scheme 3.

A solution of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (1) (VII) (0.20 g, 0.57 mol) in SOCl₂ (5 mL) was heated under reflux in N₂ for 84 h. Excess SOCl₂ was removed under reduced pressure, and the residue was chromatographed on silica gel. Elution with EtOAc/petroleum ether (3:7) gave 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzonitrile (7) (Ic: X═Cl, R═CN) (0.16 g, 87%), mp (CHCl₃) 127° C. ¹ H NMR (CD₃ COCD₃) δ 8.79 (s, 1 H, H-3), 8.19 (s, 1 H, H-6), 3.93 (s, 8 H, NCH₂ CH₂ Cl). ¹³ C NMR δ 148.55 (C-5), 140.98, 139.07 (C-2,4), 129.50, 126.10 (C-3,6), 115.05 (C-1), 112.84 (CN), 54.18 (CH₂ N), 42.20 (CH₂ Cl). Anal. (C₁₁ H₁₀ Cl₂ N₄ O₄) C,H,N.

A solution of (1) (VII) (0.50 g, 1.42 mmol) in p-dioxane (20 mL) was treated with P₂ S₅ (0.63 g, 2.84 mmol) and NaHCO₃ (0.24 g, 2.84 mmol) was heated under reflux with stirring for 3 h. The residue after workup was chromatographed on silica gel, and elution with EtOAc/petroleum ether (1:4) gave 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrothiobenzamide (13) Ic: X═Cl, R═CSNH₂) (0.48 g, 92%), mp (EtOAc/petroleum ether) 166°-167° C. ¹ H NMR (CD₃ SOCD₃) δ 9.50, 9.34 (2xbr, 2 H, CSNH₂), 8.50 (s, 1 H, H-3), 7.45 (s, 1 H, H-6), 3.87, 3.82 (2xm, 8 H, NCH₂ CH₂ Cl). ¹³ C NMR δ 199.46 (CS), 148.08 (C-5), 143.87 (C-1), 139.51, 136.99 (C-2,4), 125.23, 121.36 (C-3,6), 54.23 (CH₂ N), 42.02 (CH₂ Cl). Anal. (C₁₁ H₁₂ Cl₂ N₄ O₄ S) C,H,N,S.

EXAMPLE D Preparation of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzenesulfonamide (18) (Id: X═Cl, R═SO₂ NH₂) by the method outlined in Scheme 4

A solution of 5-chloro-2,4-dinitrobenzenesulfonamide (VIII) [Herbert, R. B. and Hollman, R. G. Tetrahedron, 1965, 21, 663-675] (1.55 g, 5.5 mmol) and diethanolamine (1.16 g, 11 mmol) in dioxan (100 mL) was held at 60° C. for 1.5 h, then adsorbed directly onto silica gel. Excess solvent was evaporated under reduced pressure, and the residue was chromatographed on silica gel, eluting with EtOAc/MeOH (19:1), to give 5-[N,N-bis(2-hydroxyethyl)amino]-2,4-dinitrobenzenesulfonamide (IX) (1.91 g, 99%), mp (EtOAc/petroleum ether) 138°-139° C. ¹ H NMR ((CD₃)₂ SO) δ 8.53 (s, 1 H, H-3), 7.97 (s, 1 H, H-6), 7.93 (br s, 2 H, SO₂ NH₂), 4.88 (t, J=5.1 Hz, 2 H, OH), 3.65 (dt, J=5.2, 5.1 Hz, 4 H, CH₂ OH), 3.49 (t, J=5.1 Hz, 4 H, NCH₂). ¹³ C NMR δ 146.84 (C-5), 140.53 (C-1), 136.84, 134.39 (C-2,4), 125.70 (C-3), 54.27 (NCH₂). Anal. (C₁₀ H₁₄ N₄ O₈ S) C,H,N.

A stirred solution of the above diol (IX) (1.90 g, 5.43 mmol) and Et₃ N (1.90 mL, 14 mmol) in dry THF (60 mL) was treated dropwise at 0° C. with methanesulfonyl chloride (0.89 mL, 11 mmol). After a further 15 min, the solution was diluted with EtOAc, washed well with water, and worked up to give the crude dimesylate (Id: X═OSO₂ Me, R═SO₂ NH₂). This was immediately dissolved in DMF (50 mL) containing LiCl (20 g), and the mixture stirred at 130° C. for 15 min before solvent was removed under reduced pressure. The residue was partitioned between EtOAc and water, and the organic layer was worked up and chromatographed on silica gel. Elution with EtOAc gave 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzenesulfonamide (18) (Id: X═Cl, R═SO₂ NH₂) (1.47 g, 64%), mp 153°-154° C. (EtOAc/petroleum ether). ¹ H NMR ((CD₃)₂ CO) δ 8.54. (S, 1H, H-3), 7.99 (br, 2H, SO₂ NH₂), 7.91 (S, 1H, H-6), 3.84 (t, J=5.6 Hz, 4H, CH₂ Cl), 3.67 (t, J=5.6 Hz, 4H, CH₂ N). ¹³ C NMR ((CD₃)₂ CO) δ 146.13 (C-5), 140.64 (C-1), 138.86, 136.93 (C-2,4), 124.95, 121.77 (C-3,6), 52.47 (CH₂ N), 41.62 (CH₂ Cl). Anal. (C₁₀ H₁₂ Cl₂ N₄ O₆ S) C,H,N,S.

EXAMPLE E Preparation of 2-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (19) (Ie: R═CONH₂) and N-(N,N-dimethylaminoethyl) 2-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (20) (Ie: R═CONHCH₂ CH₂ NMe₂) by the method outlined in Scheme 5.

Reaction of commercially-available 2-chloro-3,5-dinitrobenzoic acid (X) with SOCl₂ gave 2-chloro-3,5-dinitrobenzoyl chloride (XI: Z═Cl), which was quenched with ammonia to give 2-chloro-3,5-dinitrobenzamide (XI: Z═NH₂). A solution of this amide (1.00 g, 4.07 mmol) and Et₃ N (1.42 g, 10 mmol) in p-dioxane (30 mL) was treated with N,N-bis(2-chloroethyl)amine hydrochloride (1.45 g, 8.14 mmol) at 50° C. for 18 h. The mixture was then poured into water and extracted with EtOAc to give an oil, which was chromatographed on silica gel. Elution with EtOAc/petroleum ether (1:1) gave 2-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (19) (Ie: R═CONH₂) (1.15 g, 80%), mp (CHCl₃ /petroleum ether) 123°-124° C. ¹ H NMR (CH₃ SOCD₃) δ 8.70 (d, J=2.7 Hz, 1 H, H-4), 8.49 (d, J=2.7 Hz, 1 H, H-6), 7.68, 7.35 (2xbr, 2H, CONH₂), 3.80, 3.61 (2xt, J=6.9 Hz, 8 H, NCH₂ CH₂ Cl). ¹³ C NMR δ 167.94 (CONH₂), 147.27 (C-2), 147.20, 142.84 (C-3,5), 137.70 (C-1), 128.40, 123.24 (C-4,6), 55.84 (CH₂ N), 42.28 (CH₂ Cl). Anal. (C₁₁ H₁₂ Cl₂ N₄ O₅) C,H,N,Cl.

Similar treatment of the acid chloride (XI: Z═Cl) with N,N-dimethylethylenediamine in water at 0° C. gave N-(N,N-dimethylaminoethyl 2-chloro-3,5-dinitrobenzamide (XI: Z═NHCH₂ CH₂ NMe₂) as a viscous oil (5.6 g, 59%. The hydrochloride salt crystallised from MeOH/isopropyl ether, mp 220°-222° C. ¹ H NMR (D₂ O) δ 8.99 (d, J=2.3 Hz, 1 H, ArH4), 8.74 (d, J=2.3 Hz, 1 H, ArH6), 3.89 (t, J=6.3 Hz, 2 H, CH₂ N⁺ Me₂), 3.51 (t, J=6.3 Hz, 2 H, CONHCH₂), 3.04 (s, 6 H, NMe₂). ¹³ C NMR 169.32 (CONH), 150.88 (C-2), 148.70, 141.02 (C-3,5), 133.23 (C-1), 129.45, 125.27 (C-4,6), 58.64 (CH₂ N⁺ Me₂), 45.88 (N⁺ Me₂), 37.94 (CONHCH₂). Anal. (C₁₁ H₁₃ ClN₄ O₅.HCl) C,H,N,Cl.

Reaction of this amide (XI: Z═NHCH₂ CH₂ NMe₂) with bis(2-chloroethyl)amine hydrochloride and Et₃ N as above, followed by chromatography on silica gel and elution with EtOAc/MeOH (9:1) gave N-(N,N-dimethylaminoethyl) 2-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (20 ) (Ie: R═CONHCH₂ CH₂ NMe₂), mp (EtOAc/petroleum ether) 115°-118° C. ¹ H NMR (CDCl₃) δ 8.63 (s, 2 H, ArH4), 7.41 (br, 1 H, CONH), 3.74 (t, J=6.3 Hz, 4 H, CH₂ Cl), 3.59 (t, J=5.8 Hz, 2 H, CONHCH₂), 3.55 (t, J=6.3 Hz, 4 H, NCH₂ CH₂ Cl), 2.56 (t, J=5.8 Hz, 2 H, CH₂ NMe₂), 2.27 (s, 6 H, NMe₂). ¹³ C NMR 164.70 (CO), 145.93 (C-2), 144.86, 141.94 (C-3,5), 135.68 (C-1), 129.63 (C-4), 123.16 (C-6), 57.51 (CONHCH₂), 54.82 (NCH₂ CH₂ Cl), 45.12 (NMe₂), 41.39 (NCH₂ CH₂ Cl), 37.67 (CONHCH₂). Anal. (C₁₅ H₂₁ Cl₂ N₅ O₅) C,H,N,Cl. (The hydrochloride salt was too hygroscopic to handle).

EXAMPLE F Preparation of 3-[N,N-bis(2-chloroethyl)amino]-2,6-dinitrobenzamide (21) (If: R═CONH₂) and N-(N,N-dimethylaminoethyl) 3-[N,N-bis(2-chloroethyl)amino]-2,6-dinitrobenzamide (22) (If: R═CONHCH₂ CH₂ NMe₂) by the method outlined in Scheme 6

A solution of 3-chlorobenzoic acid (60 g, 0.38 mol) in c.H₂ SO₄ (600 ml) was treated portionwise with fuming nitric acid (d 1.42) (150 ml), and the solution was warmed gradually with stirring to 140° C. in an open flask, and held at this temperature for 6 h. After cooling overnight, ice-water was added cautiously, and after chilling to 5° C. for 3 h the precipitated product was removed by filtration and washed well with water. Crystallisation from aqueous EtOH gave 5-chloro-2,4-dinitrobenzoic acid (II: Y═OH) (62 g, 66%) mp 180°-183° C. [Goldstein, H.; Stamm, R. Helv. Chim. Acta., 1952, 35, 1330-1332 report mp 182°-183° C.]. The original filtrate and washings were combined and allowed to stand for several hours, depositing crystals of pure 3-chloro-2,6-dinitrobenzoic acid (XII) (8.4 g, 9%), mp (H₂ O), 162°-163.5° C. ¹ H NMR (CD₃ SOCD₃) δ 10.50 (br, 1 H, COOH), 8.82 (d, J=8.8 Hz, 1 H, H-5), 8.62 (d, J=8.8 Hz, 1 H, H-4). ¹³ C NMR δ 162.03 (COOH), 146.34 (C-2), 145.57 (C-6), 133.69 (C-5), 130.01 (C-1), 128.26 (C-4), 125.19 (C-3). Anal. (C₇ H₃ ClN₂ O₆) C,H,N,Cl.

The 3-chloro-2,6-dinitrobenzoic acid (XII) was converted to the ethyl ester, which was reacted as above with diethanolamine to give crude ethyl 3-[N,N-bis(2-hydroxyethyl)amino]-2,6-dinitrobenzoate (XIII: X═OH, Z═OEt). Reaction of this with MsCl/LiCl gave ethyl 3-[N,N-bis(2-chloroethyl)amino]-2,6-dinitrobenzoate (XIII: X═Cl, Z═OEt), mp (EtOAc/petroleum ether) 84°-87° C. ¹ H NMR (CD₃ COCD₃) δ 8.32 (d, J=9.4 Hz, 1 H, H-5), 7.79 (d, J=9.4 Hz, 1 H, H-4) 4.39 (q, J=7.1 Hz, 2 H, OCH₂ CH₃), 3.85-3.77 (m, 8 H, NCH₂ CH₂ Cl), 1.34 (t, J=7.1 Hz, 3 H, OCH₂ CH₃). ¹³ C NMR δ 163.24 (COOEt), 148.30 (C-3), 141.04, 138.80 (C-2,6), 128.84, 124.65 (C-4,5), 127.39 (C-1), 63.94 (OCH₂ CH₃), 54.39 (NCH₂), 42.00 (CH₂ Cl) 13.89 (OCH₂ CH₃). Anal. (C₁₃ H₁₅ Cl₂ N₃ O₆) C,H,N,Cl.

An X-ray crystallographic determination was carried out on this compound to confirm the structure.

Hydrolysis of this ester (XIII: X═Cl, Z═OEt) in aqueous KOH/p-dioxane (30 mL) at 20° C. for 18 h gave 3-[N,N-bis(2-chloroethyl)amino]-2,6-dinitrobenzoic acid (XIII: X═Cl, Z═OH), which was converted to the corresponding acid chloride (XIII; X═Cl, Z═Cl). A solution of this in Me₂ CO at 0° C. was treated with excess aqueous ammonia, and the product was chromatographed on silica gel, EtOAc/petroleum either (1:1) eluting 3-[N,N-bis(2-chloroethyl)amino]-2,6-dinitrobenzamide (21) (If: R═CONH₂) (0.93 g), mp (EtOAc/petroleum ether) 140°-141.5° C. ¹ H NMR (CD₃ COCD₃) δ 8.26 (d, J=9.3 Hz, 1 H, H-5), 7.71 (d, J=9.3 Hz, 1 H, H-4), 7.63, 7.23 (2xbr, 2 H, CONH₂), 3.75 (s, 8 H, NCH₂ CH₂ Cl). ¹³ C NMR δ 163.99 (CONH₂), 147.38 (C-3), 142.92, 139.76 (C-2,6), 130.48 (C-1), 128.22, 124.23 (C-4,5), 54.74 (NCH₂), 42.00 (CH₂ Cl). Anal. (C₁₁ H₁₂ Cl₂ N₄ O₅) C,H,N,Cl.

Similar treatment of the acid chloride (XIII: X═Cl, Z═Cl) with N,N-dimethylethylenediamine gave N-(N,N-dimethylaminoethyl) 3-[N,N-bis(2-chloroethyl)amino]-2,6-dinitrobenzamide (22) (If: R═CONHCH₂ CH₂ NMe₂). The hydrochloride salt crystallised from MeOH/isopropyl ether, mp 180°-182° C. 1H NMR (D₂ O) δ 8.37 (d, J=9.6 Hz, 1 H, ArH5), 7.63 (d, J=9.6 Hz, 1 H, ArH4), 3.80-3.71 (m, 10 H, NCH₂ CH₂ Cl and CH₂ NMe₂), 3.44 (t, J=6.4 Hz, 2 H, CONHCH₂), 3.00 (s, 6 H, NMe₂), ¹³ C NMR δ 168.75 (CONH), 150.91 (C-3), 141.55, 138,72 (C-2,6), 131.61 (C-4), 130.45 (C-1), 125.85 (C-5), 58.31 (CH₂ N⁺ Me₂), 55.74 (NCH₂ CH₂ Cl), 45.97 (N⁺ Me₂), 44.16 (NCH₂ CH₂ Cl), 37.91 (CONHCH₂). Anal. (C₁₅ H₂₁ Cl₂ N₅ O₅.HCl) C,H,N,Cl.

EXAMPLE G Preparation of 4-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (23) (Ig: X═Cl, R═CONH₂) and N-(N,N-dimethylaminoethyl) 4-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (24) (Ig: X═Cl, R═CONHCH₂ CH₂ NMe₂) by the method outlined in Scheme 7

A solution of methyl 4-chloro-3,5-dinitrobenzoate (XIV) (10.0 g, 0.036 mol) and diethanolamine (7.66 g, 0.073 mol) in p-dioxane (60 mL) was stirred at 50° C. for 5 h. Volatiles were removed under reduced pressure, and the residue was adsorbed directly onto silica gel and chromatographed. Elution with EtOAc/petroleum ether (1:10) gave foreruns, and subsequent elution with EtOAc/petroleum ether (3:2) gave methyl 4-[N,N-bis(2-hydroxyethyl)amino]-3,5-dinitrobenzoate (XV: X═OH, Z═OMe) (9.61 g, 80%), mp (CHCl₃ /petroleum ether) 101°-103° C. ¹ H NMR (CDCl₃) δ 8.52 (s, 2 H, ArH-2,6), 3.97 (s, 3 H, COOCH₃), 3.76 (dxt, J=6.5, 4.7 Hz, 4 H, CH₂ OH), 3.26 (t, J=4.7 Hz, 4 H, NCH₂), 2.76 (t, J=6.5 Hz, 2 H, OH). ¹³ C NMR δ 163.14 (COOCH₃), 145.50 (C-4), 142.54 (C-3,5), 131.19 (C-2,6), 123.59 (C-1), 59.16 (CH₂ OH)1, 54.58 (CH₂ N), 53.14 (OCH₃). Anal. (C₁₂ H₁₅ N₃ O₈) C,H,N.

MsCl (3.93 mL, 0.049 mol) was added dropwise at 0° C. to a solution of the above diol (XV: X═OH, Z═OMe) (7.30 g, 0.022 mol) and Et₃ N (7.72 mL, 0.055 mol) in CH₂ Cl₂ (100 mL). After 15 min, the solution was washed several times with water and worked up to give the crude dimesylate, which was treated with LiCl in DMF at 120° C. for 5 min. Workup and chromatography on silica gel (elution with EtOAc/petroleum ether (1:4)) gave methyl 4-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzoate (XV: X═Cl, Z═OMe) (6.21 g, 77%), mp (CHCl₃ /petroleum ether) 93°-95° C. ¹ NMR (CDCl₃) δ 8.54 (s, 2 H, H-2,6), 3.99 (s, 3 H, COOCH₃), 3.63 (t, J=6.9 Hz, 4 H, CH₂ Cl), 3.43 (t, J=6.9 Hz, 4 H, CH₂ N). ¹³ C NMR δ 162.90 (COOCH₃), 47.83 (C-4), 140.53 (C-3,5), 129.85 (C-2,6), 126.70 (C-1), 55.47 (CH₂ N), 53.23 (OCH₃), 41.18 (CH₂ Cl). Anal. (C₁₂ H₁₃ Cl₂ N₃ O₆) C,H,N,Cl.

Hydrolysis of this ether (XV: X═Cl, Z═OMe) with aqueous KOH/p-dioxane at 20° C. for 3 h gave a quantitative yield of 4-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzoic acid (XV: X═Cl, Z═OH), mp EtOAc/petroleum ether) 164°-166° C. ¹ NMR ((CD₃)₂ SO) δ 8.61 (s, 2 H, H-2,6), 3.78 (t, J=6.9 Hz, 4 H, CH₂ Cl), 3.52 (t, J=6.9 Hz, 4 H, CH₂ N) (COOH not visible). ¹³ C NMR δ 164.12 (COOH), 149.12 (C-4), 141.40 (C-3,5), 130.70 (C-2,6), 128.19 (C-1), 56.14 (CH₂ N), 42.46 (CH₂ Cl). Anal (C₁₁ H₁₁ Cl₂ N₃ O₆) C,H,N,Cl.

The above acid (XV: X═Cl, Z═OH) was converted to the crude acid chloride (XV: X═Cl, Z═Cl), which was dissolved in dry Et₂ O (100 mL), cooled to 5° C., and treated dropwise with aqueous NH₃ (20 mL of a 3N solution, 60 mmol). After 10 min the solution was worked up, and the residue was chromatographed on silica. Elution with EtOAc/petroleum ether (3:7) gave foreruns, while EtOAc/petroleum ether (7:3) gave 4-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (23) (Ig: X═Cl, R═CONH₂) (80% overall yield), mp (EtOAc/petroleum ether) 113°-116° C. ¹ H NMR (CD₃ COCD₃) δ 8.61 (s, 2 H, H-2,6), 7.98, 7.24 (2xbr, 2 H, CONH₂), 3.75 (t, J=7.0 Hz, 4 H, CH₂ Cl), 3.50 (t, 4 H, CH₂ N). ¹³ C NMR δ 164.91 (CONH₂), 149.32 (C-4), 140.07 (C-3,5), 132.18 (C-1), 128.91 (C-2,6), 56.37 (CH₂ N), 42.55 (CH₂ Cl). Anal. (C₁₁ H₁₂ Cl₂ N₄ O₅) C,H,N,Cl.

Similar treatment of the crude acid chloride (XV: X═Cl, Z═Cl) with N,N-dimethylethylenediamine gave N-(N,N-dimethylaminoethyl) 4-[N,N-bis(2-chloroethyl)amino]-3,5-dinitrobenzamide (24) (Ig: X═Cl, R═CONHCH₂ CH₂ NMe₂). The hydrochloride salt crystallised from MeOH/isopropyl ether, mp 145°-148° C. ¹ H NMR (CD₃ SOCD₃) δ 10.65 (br, 1 H, HCl), 9.49 (t, J=5.4 Hz, 1 H, CONH), 8.75 (s, 2 H, ArH2,6), 3.71 (t, J=6.9 Hz, 4 H, NCH₂ CH₂ Cl), 3.44-3.28 (m, 8 H, NCH₂ CH₂ Cl and CH₂ CH₂ N⁺ Me₂), 2.83 (s, 6 H, N⁺ Me₂). ¹³ C NMR δ 162.63 (CO), 147.43 (C-3,5), 138.75 (C-4), 130.22 (C-1), 128.31 (C-2,6), 55.44 (CH₂ N⁺ Me₂), 54.75 (NCH₂ CH₂ Cl), 42.22 (N³⁰ Me₂), 42.18 (NCH₂ CH₂ Cl), 34.75 (CONHCH₂). Anal. (C₁₅ H₂₁ Cl₂ N₅ O₅.HCl) C,H,N,Cl.

The following Table 2 gives biological data for selected examples of the compounds listed in Table 1. The abbreviations used in Table 2 are:

    ______________________________________                                         No.    The number given the corresponding                                             compound in Table 1.                                                    IC.sub.50                                                                             Growth inhibition studies were performed                                       as described in detail elsewhere (W. R. Wilson,                                R. F. Anderson and W. A. Denny. J. Med. Chem.,                                 1989, 32, 23; G. J. Finlay, B. C. Baguley and                                  W. R. Wilson. Anal. Biochem., 1984, 139, 172.),                                using 200 viable AA8 or 300 viable UV4 cells plus                              5000 lethally-irradiated AA8 feeder cells per well in                          96-well tissue culture dishes. AA8 and UV4 cells                               were maintained in logarithmic-phase growth in 25                              cm.sup.3 tissue culture flasks with subculture                                 twice weekly by trypsinization. The growth medium                              was antibiotic-free α-MEM with 10% v/v                                   heat-inactivated (56° C., 40 min)                                       fetal calf serum. Doubling times were approximately                            14 h for AA8 and 15h for UV4 cells. Cultures were                              tested for mycoplasma contamination frequently,                                using a cytochemical staining method (I. R.                                    Chen, Exp. Cell Res., 1977, 104, 255. Drugs                                    were added 24 hours after initiating cultures in                               96-well dishes, and cells were incubated                                       under aerobic or hypoxic conditions for 18 hours                               before washing with fresh medium. The IC.sub.50                                was determined as the drug concentration                                       needed to reduce the cell mass (protein content,                               measured after 72-78h by staining with methylene                               blue and measuring absorbance in a microplate                                  photometer) to 50% of the mean value for 8 control                             cultures on the same 96-well plate.                                     HF.sub.air                                                                            Ratio of IC.sub.50 values for a compound                                       after exposure as detailed above against AA8 and UV4                           cell lines (HF = IC.sub.50 (AA8)/IC.sub.50 (UV4)).                      CT.sub.10                                                                             The product (in μM-hr) of the drug concentration                            times the exposure time to reduce cell survival to 10%                         of control values in the clonogenic assay.                              air/N.sub.2                                                                           Ratio of CT.sub.10 values after exposure of                                    UV4 cells as detailed above under either aerobic (air)                         or hypoxic (N.sub.2) conditions (= aerobic                                     CT.sub.10 /hypoxic CT.sub.10).                                          HF.sub.NR-2                                                                           Ratio of IC.sub.50 values for a compound                                       after exposure as detailed above against the UV4                               cell line in the presence and absence of the E. coli                           nitroreductase enzvme NR-2.                                             ______________________________________                                    

                                      TABLE 2                                      __________________________________________________________________________     Biological activity of selected compounds of Table 1                              IC.sub.50 (AA8)                                                                      HF  CT.sub.10 (UV4)                                                                       CT.sub.10 ratio                                                                      IC.sub.50 (UV4)                                                                       HF (NR-2)                                     No (air: μM)                                                                         (air)                                                                              (air: μM-h)                                                                        (air/N.sub.2)                                                                        (air: μM)                                                                          (air)                                         __________________________________________________________________________     1  468   6.8 2925  59    109    73.5                                           2  57    7.5 160   20    10.9   32.3                                           3  34    2.6 170   42    15     73.8                                           4  >200  --  1200  17    99     10.0                                           6  10600 1.5 >30000                                                                               >2    317    0.76                                           7  24    6.8 86    8.5   2.3    9.2                                            8  >100  --  >360  --                                                          9  310   I.4 >3500 >20                                                         10 264   23  156   1.6                                                         11 230   4.2 1130  60                                                          12 920   3.0 3700  45                                                          13 >25   >2  >60   >3                                                          14 7300  1.7 <14400                                                                               <10                                                         15 6100  1.1 14000 2                                                           17 1790  3.2 3340  14                                                          18 3     --  --    --                                                          19 >100  ca. 3                                                                              >300  >5                                                          20 150   14  1200  36                                                          21 >240  >2  >300  >3                                                          22 426   3.2 3600  130                                                         23 97    1.4 >450  >1                                                          24 62    2.0 >273  >1                                                          __________________________________________________________________________

The following Examples 1 to 3 show that compound 1 (referred to therein as SN23862) is reductively activated by bacterial nitroreductase enzymes.

The alkylating agent 5-(aziridin-1-yl)-2,4-dinitrobenzamide (hereinafter designated CB 1954) has been known, almost for 20 years, as an interesting experimental compound of unique selectivity. Although CB 1954 is structurally quite closely related to numerous other known alkylating agents which have a relatively broad range of activity, CB 1954 exhibits considerable activity against the Walker tumour cells in vivo or in vitro but was thought to be virtually inactive against other tumours.

It was recently discovered that the selectivity of CB 1954 arose from the fact that it was not an anti-tumour agent per se but was a prodrug for an anti-tumour agent generated from CB 1954 by a nitroreductase enzyme found in the Walker cell. This nitroreductase from the Walker cell was subsequently shown to be an enzyme known from other sources which was an NAD(P)H dehydrogenase (quinone) classified as EC.1.6.99.2, see Robertson et al, J. Biol. Chem. 261, 15794-15799 (1986).

In the course of the previous investigations with CB 1954, it was found that the Walker cell enzyme EC.1.6.99.2 had the ability to reduce the 4-nitro group of CB 1954 to the corresponding hydroxylamine and that it was the resulting 5-(aziridin-1-yl)-2-nitro-4-hydroxylamino-benzamide that was the active anti-tumour agent.

PCT Application PCT/GB92/01947 of Cancer Research Campaign Technology Limited describes new nitroreductases, obtainable from bacterial sources, for example from Escherichia coli and from Bacillus amyloliquifaciens, that are of interest in that not only are they capable of converting CB 1954 into an active anti-tumour agent, but also, unlike EC.1.6.99.2. capable of converting CB 1954 analogues which are also prodrugs into active anti-tumour agents.

As is more particularly described in PCT Application PCT/GB92/01947 the use of prodrugs represents a clinically very valuable concept in cancer therapy since, particularly where the prodrug is to be converted to an anti-tumour agent under the influence of an enzyme that is linkable to a monoclonal antibody that will bind to a tumour associated antigen, the combination of such a prodrug with such an enzyme monoclonal/antibody conjugate represents a very powerful clinical agent.

    ______________________________________                                                                     % DRUG                                             TREATMENT       % SURVIVAL  REDUCTION                                          ______________________________________                                         CONTROL         100         --                                                 +500 μM NADH 100         --                                                 +50 μM SN23862                                                                              100         <1.0                                               +NADH + SN23862 100         <1.0                                               +Nitroreductase 94          --                                                 +NR + 50 μM SN23862                                                                         99          <1.0                                               +NR + SN23862 + 0.007       95                                                 500 μM NADH                                                                 ______________________________________                                    

    ______________________________________                                                                     % DRUG                                             TREATMENT       % SURVIVAL  REDUCTION                                          ______________________________________                                         CONTROL         100         --                                                 +500 μM NADH 120         --                                                 +50 μM SN23862                                                                              110         <1.0                                               +NADH + SN23862 115         <1.0                                               +Nitroreductase 96.8        --                                                 +BA + 50 μM SN23862                                                                         110         <1.0                                               +BA + SN23862 + 6.0         >95                                                500 μM NADH                                                                 ______________________________________                                    

    __________________________________________________________________________                       % SURVIVAL                                                   TREATMENT         MAWI Cells                                                                            V79 Cells                                                                            % DRUG REDUCTION                                __________________________________________________________________________     CONTROL           100    100   --                                              +500 μM NADH   104.6  94.6  --                                              +50 μM SN23862 90.9   94.3  <1.0                                            +NADH + SN23862   93.1   80.4  <1.0                                            +Conjugate (CG)   85.5   85.8  --                                              +CG + 50 μM SN23862                                                                           94.6   73.5  <1.0                                            +CG + SN23862 + 500 μM NADH                                                                   0.014  0.003 >99                                             __________________________________________________________________________

BRIEF DESCRIPTION OF DRAWING

The accompanying FIG. 1 shows radiosensitising properties of compound 1.

The radiosensitising efficiency of compound 1 has been assessed in stirred suspensions of AA8 cells under hypoxic conditions using gamma irradiation (cobalt 60) at a dose rate of 2.2 Gy/min at 37° C. Drug and cells were mixed under hypoxic conditions 30 min before irradiation. Radiosensitisation of hypoxic cells was observed (FIG. 1). The concentration for an enhancement ratio (ratio of radiation doses for 10% survival with and without drug) of 1.6 (C₁.6) was approximately 100 μM, and this extent of sensitisation was observed in the absence of drug toxicity (FIG. 1). Compound 1 is therefore a hypoxic cell radiosensitiser as well as a hypoxia-selective cytotoxin.

It is clear from the data of Table 2, Examples 1 to 3 and FIG. 1 that the examples of the nitroaniline derivatives of general formula (I) listed in Table 2 include compounds which are active as cytotoxic agents, and which have the additional capability of being reductively activated by both mammalian tumour cells and bacterial nitroreductase enzymes, and are therefore suitable as prodrugs. The compounds are selectively toxic to hypoxic tumour cells, and therefore useful as anticancer drugs. The compounds are capable of sensitising hypoxic cells in vitro to ionising radiation, and thus are suitable as hypoxic cell radiosensitisers.

The present invention therefore also provides pharmaceutical compositions, having antitumour and radiosensitising activity, and comprising at least one compound represented by the general formula (I), and one or more pharmaceutically-acceptable carriers or diluents.

The present invention further provides the use of at least one compound represented by the general formula (I) for the manufacture of pharmaceutical compositions for the treatment of tumours, in particular cancers.

When the compounds of formula (I) are used as reductively-activated prodrugs for cytotoxins, they can be used in association with nitroreductase enzymes, including the nitroreductases described in Application PCT/GB92/01947, and so provide a system of cancer chemotherapy where the extent of exposure of the patient to the cytotoxic agent is limited, so far as possible, to those regions where there is the inter-reaction between the prodrug and the nitroreductase.

The most or one of the most convenient ways of utilising such a system of cancer chemotherapy is to conjugate the nitroreductase to a targeting agent such as a monoclonal antibody that will bind with a tumour-associated antigen.

The term "monoclonal antibody" will be understood by those of skill in the art not simply to refer to antibodies produced by traditional hybridoma techniques, but also to cover antibodies and variants thereof produced by recombinant means. These include, for example, humanised antibodies such as those with a constant region from a human antibody grafted onto a non-human antibody variable region (see for example EP-A-0 120 694), chimeric antibodies such as those with non-human complimentarily determining regions (CDRs) grafted into a human variable region framework (see for example EP-A-0 239 400) and single chain antibodies. Fragments of such monoclonal antibodies which retain their target binding activity are also included by the general term "monoclonal antibody". This includes Fab' and F(ab')₂ fragments.

The selection of monoclonal antibody will clearly be influenced by the nature of the target tumour but for the purposes of illustration, reference may be made to the anti-CEA antibody A₅ B₇.

With this system, it is possible in a course of cancer chemotherapy to administer to the patient requiring the treatment the nitroaniline compound which is the prodrug for a cytotoxic compound and the enzyme/targeting agent conjugate. The prodrug and the conjugate can be administered simultaneously but it is often found preferable, in clinical practice, to administer the enzyme/agent conjugate before the prodrug; e.g. up to 72 hours before, in order to give the enzyme/agent conjugate an opportunity to localise in the region of the tumour target. By operating in this way, when the prodrug is administered, conversion of the prodrug to the cytotoxic agent tends to be confined to the regions where the enzyme/agent conjugate is localised, i.e. the region of the target tumour and damage to healthy cells caused by the premature release of the cytotoxic agent is minimised.

The degree of localisation of the enzyme/agent conjugate (in terms of the ratio of localized to freely circulating active conjugate) can be further enhanced using the clearance and/or inactivation systems described in WO89/10140. This involves, usually following administration of the conjugate and before administration of the prodrug, the administration of a component (a "second component") which is able to bind to the such part of the conjugate so as to inactivate the enzyme and/or accelerate the clearance of the conjugate from the blood. Such a component may include an antibody to the nitroreductase which is capable of inactivating the enzyme.

The second component may be linked to a macromolecule such as dextran, a liposome, albumin, macroglobulin or a blood group O erythrocyte so that the second component is restrained from leaving the vascular compartment. In addition or as an alternative, the second component may include a sufficient number of covalently bound galactose residues, or residues of other sugars such as lactose or mannose, so that it can bind the conjugate in plasma but be removed together with the conjugate from plasma by receptors for galactose or other sugars in the liver. The second component should be administered and designed for use such that it will not, to any appreciable extent, enter the extravascular space of the tumour where it could inactivate localised conjugate prior to and during administration of the prodrug.

The exact dosage regime will, of course, need to be determined by individual clinicians for individual patients and this, in turn, will be controlled by the exact nature of the prodrug and the cytotoxic agent to be released from the prodrug but some general guidance can be given. Chemotherapy of this type will normally involve parenteral administration of both the prodrug and the enzyme/agent conjugate and administration by the intravenous route is frequently found to be the most practical.

The active compounds may be orally administered, for example, with an inert diluent or with an assimilable edible carrier, or they may be enclosed in hard or soft shell gelatin capsules, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet. For oral therapeutic administration, the active compounds may be incorporated with excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers and the like. Such compositions and preparations should contain at least 0.1% of active compound. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2 and about 60% of the weight of the unit. The amount of active compound in such therapeutically useful compositions is such that a suitable dosage will be obtained. Preferred compositions or preparations according to the present invention are prepared so that an oral dosage unit form contains between about 5 and about 200 mg of active compound.

The tablets, troches, pills, capsules and the like may also contain the following: a binder such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, lactose or saccharin may be added or a flavouring agent such as peppermint, oil of wintergreen or cherry flavouring. When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills or capsules may be coated with shellac, sugar or both. A syrup or elixir may contain the active compound, sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavouring such as cherry or orange flavour. Of course any material used in preparing any dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed. In addition, the active compounds may be incorporated into sustained-release preparations and formulations.

The active compounds may also be administered parenterally or intraperitoneally. Solutions of the active compound as a free base or pharmaceutically acceptable salt can be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against be contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, clorobutanol, phenol, sorbic acid, thimerosal and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminium monostearate and gelatin.

Sterile injectable solutions are prepared by incorporating the active compound in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and the freeze-drying technique which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

As used herein, "pharmaceutically acceptable carrier" includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents and the like. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions.

It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suitabale as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined therapeutic effect in association with the required pharmaceutical carrier. The specification for the novel dosage unit forms of the invention are dictated by and directly dependent on (a) the unique characteristics of the active material and the particular therapeutic effect to be achieved, and (b) the limitations inherent in the art of compounding such an active material for the treatment of disease in living subjects having a diseased condition in which bodily health is impaired.

The principal active ingredient is compounded for convenient and effective administration in effective amounts with a suitable pharmaceutically-acceptable carrier in dosage unit form as hereinbefore disclosed. A unit dosage form can, for example, contain the principal active compound in amounts ranging from about 0.1 to about 400 mg, with from about 1 to about 30 mg being preferred. Expressed in proportions, the active compound is generally present in from about 0.1 to 400 mg/ml of carrier. In the case of compositions containing supplementary active ingredients, the dosages are determined by reference to the usual dose and manner of administration of the said ingredients. 

What we claim is:
 1. A compound represented by the general formula (I), ##STR4## where the nitro group is substituted at any one of the available benzene positions 2-6; where R and A separately represent the groups NO₂, CN, COOR¹, CONR¹ R², CSNR¹ R² or SO₂ NR¹ R² and A is substituted at any one of the available benzene positions 2-6; where B represents N(CH₂ CH₂ halogen)₂ or N(CH₂ CH₂ OSO₂ R³)₂ substituted at any one of the available benzene positions; and where R¹, R² and R³ separately represent H, or lower alkyl optionally substituted with hydroxyl, ether, carboxy or amino functions, including cyclic structures, or R¹ and R² together with the nitrogen form a heterocyclic structure.
 2. A compound of formula (I) according to claim 1, where NO₂ is in the 2-position, R represents CONH₂, A represents 4-NO₂ and B represents 5-N(CH₂ CH₂ Cl)₂.
 3. A compound of formula (I) according to claim 1, where NO₂ is in the 2-position, R represents CONH₂, A represents 4-NO₂ and B represents 5-N(CH₂ CH₂ Br)₂.
 4. A compound of formula (I) according to claim 1, where NO₂ is in the 2-position, R represents CONH₂, A represents 4-NO₂ and B represents 5-N(CH₂ CH₂ I)₂.
 5. A compound of formula (I) according to claim 1, where NO₂ is in the 2-position, R represents CONH₂, A represents 6-NO₂ and B represents 5-N(CH₂ CH₂ Cl)₂.
 6. A compound of formula (I) according to claim 1, where NO₂ is in the 3-position, R represents CONH₂, A represents 5-NO₂ and B represents 2-N(CH₂ CH₂ Cl)₂.
 7. A process for the preparation of a compound represented by the general formula (I) as defined in claim 1, which process is outlined at any one of Schemes 1-7 herein.
 8. A compound represented bvy the general formula (I) as defined in claim 1 prepared by a process outlined in claim
 7. 9. A pharmaceutical composition with comprises at least one compound represented by the general formula (I) as defined in claim 1, and one or more pharmaceutically-acceptable carriers or diluents. 